Quality control inspector jobs in Manchester, NH - 327 jobs

Quality Inspector III - Weekdays About Us Founded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, our client is reshaping how the world manufactures critical products. They build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through vertically integrated capabilities, including scalable additive manufacturing and precision machining, they deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Their team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. They foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because diverse perspectives lead to better outcomes. Job Purpose As a Quality Inspector III at our client, you will work in a diversified role within the Quality Inspection team dedicated to ensuring every product delivered meets the highest standards of precision, safety, and reliability. By applying expertise in inspection methods, quality systems, and problem-solving, this role safeguards customer trust, drives continuous improvement, and supports innovation in metal additive manufacturing. This position operates on the weekday shift: Monday-Friday, 6:00 AM to 2:30 PM. Key Responsibilities Perform First Article Inspections (FAI) and routine part inspections using calipers, micrometers, and other gauges. Verify that materials, equipment, processes, and products comply with quality specifications. Develop and validate inspection and test methods; assist in creating SOPs and inspection protocols. Monitor, analyze, and report on product quality metrics. Support compliance with customer, internal, and industry requirements (AS9100, ISO 9001, ISO 13485) through audits and gap analysis. Assist in developing and implementing process controls, corrective actions, and continuous improvement initiatives. Ensure workflows, processes, and products comply with safety regulations. Investigate and troubleshoot product or production issues. Inspect manufactured parts, issue non-conformance reports, and facilitate MRB hardware disposition and corrective action tasks. Work independently and manage daily priorities with minimal supervision. Communicate and collaborate with operations personnel to ensure production needs are met. Initiate and communicate identified nonconformances. Qualifications 5+ years of experience performing part inspections with strong drawing interpretation skills. Extensive knowledge of GD&T principles. Experience with First Article Inspections (FAI), Test Method Validation (TMV), and developing inspection methods. Proficiency in AQL sampling techniques. Skilled in performing dimensional and visual inspections. Experience with root cause analysis, data analysis, and troubleshooting. Experience in medical device, aerospace, or defense manufacturing required. Hands-on experience with advanced inspection equipment and software, including CMMs, PCMMs, vision systems, profilometers, and blue-light scanners (e.g., Zeiss, Faro, Keyence). Ability to troubleshoot issues encountered with inspection equipment. Self-motivated, hands-on team player with excellent communication skills; adaptable to fast-paced environments and excited by new challenges in metal additive manufacturing.

The Middlesex Corporation is a nationally recognized and award-winning leader in the heavy civil construction industry. Since 1972, the family business founded by Robert W. Pereira has developed an extensive client and project list through its consistent efforts to safely build America's infrastructure. The Middlesex Corporation specializes in building and reconstructing highways, bridges, marine, rail, and transit facilities through its collaborative team approach and focus on core values. In addition, Middlesex Asphalt in Central Florida is one of the largest and most productive asphalt plants in the United States with Middlesex Paving earning an equally solid regional presence and reputation. Position Summary: The MRM Quality Control Technician is responsible for ensuring the quality, consistency, and compliance of ready mixed concrete and aggregates produced by Massachusetts Ready Mix. This role performs routine plant and field testing, inspections, and documentation to verify materials meet applicable job specifications, Department of Transportation requirements, and industry standards. PI53309b218c6b-37***********9

The Equipment Qualification Technician is responsible for verifying, qualifying, and maintaining the quality and performance of manufacturing equipment (not finished products). This role focuses on ensuring machines and production systems operate reliably, meet qualification standards, and comply with regulatory requirements in a manufacturing environment. Key Responsibilities: Perform IQ, OQ, and PQ on manufacturing equipment Verify machine performance, functionality, and compliance (not product inspection) Document qualification results, deviations, and corrective actions Work hands-on on the manufacturing floor / shop environment Support equipment setup, troubleshooting, and issue resolution Work around production lines, machines, and industrial systems Partner with Engineering, Quality, and Operations teams Participate in root cause analysis, audits, and process improvement activities Train operators and provide technical support once equipment is qualified Experience Prior experience in a manufacturing environment (required) Experience working with machines, equipment, or production lines Experience in regulated environments (GMP / ISO preferred) Technical Skills Equipment qualification or validation exposure (IQ/OQ/PQ preferred) Mechanical aptitude with hands-on troubleshooting and equipment setup Ability to follow and document technical procedures

**Fall 2026 Co-Op - MES and Quality - Burlington, MA** As a **Fall 2026 Co-Op - MES and Quality Co-Op** ** ** in **Burlington, MA** at Keurig Dr Pepper (KDP), you will be a part of the beverage revolution. You will be working in a fast-paced, highly technical manufacturing environment that produces some of KDP's most popular beverages. Each co-op will lead high-impact projects and will be provided with opportunities to grow professionally. Come learn what it takes to succeed at an industry-leading company and help contribute to our ongoing success. You will be able to directly participate in the implementation of new technology that improves our manufacturing process. **Shift/Schedule:** + The KDP 2026 Fall Co-op Program will run from July 13 - Decemeber 11, 2026 + Full-time; 40 hours per week + Monday-Friday + 8:00am until 5:00pm + In-Person **As a Co-op you will:** + Gain knowledge in executing operational plans and projects, including data analytics and developing visualizations for DMS (Daily Management Systems) and QMS(Quality Management Systems). + Participate in AGILE project management and lead the development, verification, and testing of Data Analytics dashboards and visualization tools. + Influence software capabilities to achieve six sigma quality performance and enhance Quality Management System. + Assist with TPM (Total Productive Maintenance) implementation and Lean activities, including participation in Continuous Improvement or Kaizen events. + Test and verify new technology systems implemented for the Quality management and Manufacturing process. **Elements of the KDP Co-op Program include:** + Engaging and partnering on innovative projects to gain experience in a challenging, cross functional team environment + Participate in meet & greets and lunch & learns with KDP executives and other organization leaders + Receive professional development training such as networking, professional skills development and presenting + Be paired with a mentor to enhance your knowledge of other parts of the business and build your network + Complete a project from start to finish and present it and your takeaways to your team, department vice president and other KDP stakeholders **Total Rewards:** + $31/hour + Paid bi-weekly + $5,000 Sign-on Bonus, paid within first 30 days of employment **Requirements:** + Must be an undergraduate currently enrolled in a full-time academic program from an accredited college or university, majoring in Information Technology, Computer Science, Analytics, Engineering or another related field + Available to work 40 hours per week (M-F, 8am-5pm) + Excellent organizational skills and attention to detail with a demonstrated ability to manage multiple projects, prioritize requests, and meet deadlines + Strong communication skills including excellent listening, written, and verbal abilities + Ability to work cross-functionally, be independently driven, and a self-starter + Strong skills in Microsoft Excel and PowerPoint **Please note:** You must be work authorized in the United States on a full time basis without the need for employer sponsorship now or in the future. The Company cannot offer employment to F-1 (student) visa holders who require employer sponsorship in the future or cannot work now on a full time basis. We incorporate HireVue, an automated interview tool, into our campus recruitment process. Please visit this link (************************************************** to learn more about HireVue and how to prepare. *We recommend checking with your campus career center for additional preparation resources such as InterviewStream, Big Interview and more **Company Overview:** Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partners brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work. Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law. **A.I. Disclosure:** KDP uses artificial intelligence to assist with initial resume screening and candidate matching. This technology helps us efficiently identify candidates whose qualifications align with our open roles. If you prefer not to have your application processed using artificial intelligence, you may opt out by emailing your resume and qualifications directly to **************** . Keurig Dr Pepper is an equal opportunity employer and affirmatively seeks diversity in its workforce. Keurig Dr Pepper recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law.

Quality Inspector Amphenol Ardent Concepts is a leading designer and manufacturer of high performance multicoax and coaxial assemblies, connectors, and sockets used in the development of next generation semiconductors and electronics systems. Our core technology is the smallest, fastest, most electrically efficient compression mount connector technology worldwide. As data rate requirements increase and devices and systems shrink, Ardent's products deliver superior signal integrity in a dense footprint that can be reusable across programs to maximize cost savings. RESPONSIBILITIES: The Quality Inspector performs incoming, in process, mechanical and final inspection tasks as assigned. The Quality Inspector performs a wide variety of inspection tasks involving a RAM Optical Vision System and associated hand tools recording results against a defined specification. The inspector determined acceptability and recommends disposition of defective items in accordance with the defined procedures. o Incoming Quality Inspection of components, assemblies, and raw materials utilizing RAM Optical Vision System and general hand tools per the specification assigned. o Perform final inspection on outgoing finished goods and prepare documentation when required. o Process non-conformances and help the MRB team to disposition as required. o Organize and document inspection results and non-conformances. o Communicate directly with vendors, engineering, and purchasing to discuss quality related items. o Assist in vendor specific quality metrics and vendor audits when required. SKILLS & QUALIFICATIONS: o The ideal candidate will have two years Inspection experience o Strong GD&T (General Dimension and Tolerances) a plus o Knowledge of general quality techniques, root cause analysis, and sampling plans. o Ability to read specifications, Solid Works familiarity a plus o Knowledge of measurement equipment, RAM Optical, tools, and gauges o Advanced Personal Computer Skills o Strong communication skills both written and oral o A self-starter who uses initiative and problem identification to find solutions. o Ability to lift up to 70 pounds.

DEKA R&D has an immediate opening for a Quality Control Inspector to work in a dynamic Medical Device Research and Development company. This position is a highly visible role with significant and direct impact on the development and success of multiple engineering projects. Responsibilities as a Quality Control Inspector: Interpret Mechanical and Electrical print reading and apply inspection best practices Operate CMM equipment and utilize various measuring tools for inspection of medical device components Communicate effectively and promptly across multiple projects to provide feedback on inspection of parts Inspect various mechanical and electrical components and assemblies through incoming inspection Interpret ASME Y14.5 and GD&T standards throughout the inspection process for compliance and best practices Provide feedback on inspection activities to improve efficient whether individually or in a cross-functional setting To be successful as a Quality Control Inspector, you will need the following qualifications: 3+ years of experience in a regulated industry CMM programming, Metrology and/or CQI certified is a plus Basic GD&T knowledge required, Advanced GD&T knowledge preferred Proficient with mechanical measuring equipment such as micrometers, calipers, optical comparator Ability to operate CMMs following precise instructions Inspection of soldered components and Printed Circuit Board (PCB) assemblies; IPC-A-610 certification preferred Computer skills and knowledge; ability to learn new software (Experience with Jira is a plus) About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

Working at Freudenberg: We will wow your world! Responsibilities: Measure and record product quality using, visual, mechanical and optical gauging instruments. Inspect incoming raw material to insure that all quality requirements have been met per acceptance activities and material specifications. Ensure conformance to certifications for all materials and components received. Identify and segregate non-conforming material for material review board (MRB) disposition Generate NCMR's and assign owners. Participate in Gauge R&R's Perform applicable materials testing per acceptance activities and/or specification. Strong knowledge of interpreting drawings, customer specification, test methods, and inspection criteria. Maintain complete, legible, and accurate records. Independently handle problems that arise within area of responsibility. Knowledge of cGMP's. Knowledge of scheduling methods and ability to change priorities when directed by Supervisor/Manager. Interact effectively with other employees within the department and the company. Release product to next location upon completion within SAP system. Qualifications: High School/Trade School Diploma or GED 1-2 years of experience in Quality Control Experience in the medical device industry preferred The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Medical LLC

Were seeking a Quality Mechanical Inspector to perform detailed, accurate mechanical inspections-including FAIs, Gage R&R, OQ, PQ, and IQ-to strict drawing requirements and established quality standards. This role is highly detail-oriented and requires precision, hands-on metrology experience, and the ability to document results clearly. Youll work with CMM (Hexagon PC-DMIS), optical comparator, OGP, and traditional inspection tools (calipers, micrometers, height gages, pin gages, tool mics), and complete visual inspections to established standards. Key Responsibilities Perform dimensional and visual inspections using CMM, optical comparator, calipers, micrometers, height gages, and other metrology tools. Accurately document inspection results per company inspection procedures (e.g., TechNH standards if applicable). Write basic CMM programs to measure parts for FAIs, CPKs, PQs, OQs, and IQs. Conduct FAIs and Gage R&R, as well as PQ, OQ, and IQ inspections. Utilize standardized CMM fixturing based on part geometry. Interpret ballooned customer drawings with a basic understanding of GD&T. Maintain an accurate library of programs and written setup instructions for all CMM and OGP programs. Qualifications Required: Minimum 1 year experience as a mechanical inspector. Minimum 1 year CMM experience; ability to create basic CMM programs (Hexagon PC-DMIS knowledge required). Proficiency with optical comparators, tool mics, pin gages, and related tools. Basic understanding of GD&T measurements. Proficient in Microsoft Excel and MS Office. Ability to read blueprints, inspection reports, and quality documentation. Strong communication skills; ability to work independently with minimal supervision and collaborate with engineers, shift supervisors, and machine technicians. Demonstrated ability to work effectively in a multi-discipline, collaborative environment. Experience in QMS/Regulatory environments. Preferred: Experience writing basic programs for OGP systems. Familiarity with CPK studies and data reporting. Strong presentation and reporting skills. What Youll Bring High attention to detail and a commitment to accuracy. Ability to take direction well and carry out instructions competently. A team-first mindset and clear, professional communication.

JOIN AN INDUSTRY LEADER! Quality First & Green Always Sloan is the world's leading manufacturer of commercial plumbing systems and has been in operation since 1906. We are at the forefront of the green building movement and provide sustainable restroom solutions. We manufacture water- efficient products including flush valves, electronic faucets, soap dispensing and sink systems along with vitreous china fixtures for commercial, industrial and institutional markets worldwide. About the Role: We have an opening for a Quality Control Inspector II position based out of our Andover, MA location and will report to our VP of Global Quality Assurance. The Quality Control Inspector II will test and inspect components and finished devices as defined by work instructions and/or engineering specifications. This role will also report non-conformances, monitor critical equipment and instrumentation to ensure proper orientation and calibration, and complete first article inspection. What you'll do: * Inspect / test production components and subassemblies in accordance with procedures, specifications and mechanical drawings. * Perform First Article Inspections. * Perform final product inspection and test. * Maintain calibration program - monitor / track critical equipment and instrumentation for all departments to ensure proper orientation and calibration, coordinate with outside calibration house, maintain records and perform in house calibrations. * Maintain and post inspection results in quality inspection database. * Assist in writing and updating inspection procedures, protocol and checklists. * Assist shipping department by receiving parts after normal hours. * Communicate with suppliers for miscellaneous quality items - i.e. material certifications, dimensional issues. * Participate in root cause analysis and report on findings. * Other duties and responsibilities as required. What we're looking for: * High School Diploma or GED * 4+ Years Relevant Experience * 4+ Years Gage calibration * 4+ Years Layout inspection using GD&T * Basic math skills. * Demonstrates clear, professional, and respectful verbal and written communication in all interactions, consistent with an inclusive work environment. * General experience working with Microsoft Word. * General experience working with Microsoft Excel. * General experience working with 3D CAD software, CMM and/or optical comparator * Mechanical aptitude. * Must have ability to effectively communicate in English including reading, writing, speaking and listening. * Technical training required in lieu of Associate Degree * Working knowledge or measuring instruments such as CNC video measuring systems, calipers, comparator, DMM, pin gages, force gage, drop indicator, surface tester, gage blocks, depth gage, durometer and thread gages. A plus, but not required: * Associate Degree * Hazardous Waste & USDOT Hazardous Materials * Power Industrial Truck * General experience working with SAP ERP Business System * Experience with power tools such as drill press Why you'll love working here: Inclusive Culture: YOU Belong at Sloan. At Sloan, we are committed to fostering an inclusive and diverse workplace where diverse backgrounds and perspectives are embraced and celebrated. We proudly offer equal employment opportunities regardless of race, color, religion, sex, sexual orientation, gender identity and expression, national origin, disability, age, genetic information, marital status, political affiliation, veteran status, or any other characteristic protected by law. Growth Opportunities: We invest in our employees' professional development with ongoing training and career advancement opportunities. Innovative Projects: Be part of exciting projects that push the boundaries of technology and have make a real difference in the world. Compensation: The compensation range for this U.S.-based position is $62,370 - $69,300 annually. Our compensation range reflects our good faith estimate of what an ideal candidate can expect, but final agreed upon compensation will always be based on the individual candidate's experience, skills, qualifications, and other job-related or market factors that may prove relevant during the hiring process. Benefits: * Comprehensive Health Coverage: Medical (including prescription coverage), Dental, and Vision Insurance, effective the first of the month following your hire date. * Health Savings Account (HSA): With company contributions for most medical plan options. * Financial Security: Basic Life, Basic Accidental Death and Dismemberment, Short-term Disability, Long-term Disability, and Accident Insurance. * Additional Protection: Optional Life, Critical Illness, Hospital Indemnity, Legal, Pet Insurance, and Identity Theft Protection. * Convenient Commuter Benefits: Save on your daily commute. * Flexible Spending Accounts: Dependent Care FSA to help manage your expenses. * Wellness Support: Employee Assistance Plan and Wellness Programs to keep you healthy and happy. * Retirement Savings: 401(k) Retirement Savings Plan with a company match and immediate vesting. * Generous Time Off: Paid Holidays, Volunteer Time Off, Paid Time Off, Sick Leave, Military Leave, Parental Leave, Bereavement Leave, and other paid or unpaid state/local leaves where required. * Work-Life Balance: Hybrid Work Program to support your flexibility. * Employee Referral Program: Earn rewards for referring great talent. * Professional Development: Tuition Reimbursement Program to help you grow your skills. * Community and Networking: Join our Employee Business Groups and connect with colleagues. We Are Proud Partners With the Chicago Cubs We are a Legacy Partner of the Chicago Cubs and we are proud to be the organization's official water efficiency partner! Through this relationship, which includes the naming rights to Sloan Park, the Cubs' Spring Training facility in Mesa, Arizona, we have had the opportunity to promote our brand and continue our water conservation efforts in the city of Chicago and around the world. JOIN AN INDUSTRY LEADER! For additional company information please visit our website at

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. Biogen's Decision & Quality Analytics Innovation (DQAI) team is part of the Research Development & Medical (RDM) organization. The vision of the DQAI team is to drive data-driven insights from trusted data, and our team mission is to maximize the quality, efficiency and application of analytics across RDM Portfolio and Quality Management Systems through improved data and metrics management, optimization opportunities, identification of compliance risk, and enhanced business analytics application. Specifically, the DQAI team has four major focus areas: Data Management Advanced Analytics Business Intelligence Metrics Management (Performance Measurement) What You'll Do: Leverage modern AI assistants (Azure OpenAI / Copilot, GenAI-powered BI, etc.) to accelerate data exploration, automate repetitive tasks, and enhance insight storytelling. Analyze complex data from various sources to identify trends, gaps, risks, and opportunities. Work with senior staff to translate business questions into analytical problems and convert analytical outputs into actionable recommendations. Apply statistical and machine learning techniques to uncover root causes, patterns, and predictive indicators. Deliver concise insight summaries, written reports, and presentations that highlight implications and recommendations. Work with data engineering and governance teams to ensure data readiness and integrity for analytics. Support initiatives to accelerate insight discovery from portfolio analytics modeling. Develop and prototype data visualizations and dashboards. Participate in skill-building and capability-enhancement initiatives within the DQAI team. Example projects may include: Support development of custom-tailored strategic analytics solutions to answer complex questions from senior leadership. Pioneer new approaches for displaying data to engage stakeholders. Perform quality control functions to ensure the integrity of the team's work. Who You Are: You are a tech- and AI-forward problem solver who thrives on exploration and rapid iteration in a fun, collaborative team. You partner seamlessly with business stakeholders and our embedded AI developers to turn needs into analytics products and automation. Here are some of the core characteristics we're looking for: Strong analytical and critical thinking skills with a proven track record of turning data into strategic insights. Proficiency in data analysis tools and languages (e.g., Python, R). Experience applying advanced analytics, such as statistical modeling, clustering, or NLP, to real-world business challenges. Exceptional written and verbal communication skills, including the ability to synthesize complex findings for non-technical stakeholders. Ability to work collaboratively in a cross-functional environment and lead analytics initiatives from concept to insight delivery. To participate in the Biogen Internship or Co-op Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date. Be currently enrolled in an accredited community college, college, university or skills program/apprenticeship. Education Requirements Currently pursuing a Master's degree in Data Science, Statistics, Bioinformatics, Computer Science, Computational Biology, or related field Job Level: Internship Additional Information The base compensation range for this role is: $29.00-$29.00 The actual hourly wage offered will consider the candidate's current academic level and degree candidacy, inclusive of Associate, Bachelor's, Master's, JD, MD, PhD and MBA programs. It will comply with state or local minimum wage requirements specific to the job location. In addition to compensation, Biogen offers a range of benefits designed to support our educational employees, including, but not limited to: Company paid holidays Commuter benefits Employee Resource Groups participation 80 hours of sick time per calendar year Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Summary: The Lead Housing Quality Standard (HQS) Inspector is responsible for conducting any mandatory inspection for all leased units under the Rental Assistance Program in accordance to the Department of Housing and Urban Development (HUD) and Department of Housing and Community Development (DHCD) program guidance. As the Lead HQS Inspector the incumbent is expected to assist the Inspections' Supervisor in providing training to newly hired inspectors and with administrative duties as assigned. Why Work for SMOC? Paid Time Off: All full-time employees can accrue up to 3 weeks of vacation, and 2 weeks of sick time and are eligible for 12 paid holidays during their first year of employment. Employer-paid Life Insurance & AD&D and Long-Term Disability for full-time employees. Comprehensive Benefits Package including Medical Plans through Mass General Brigham with an HRA Employer cost-sharing program, Dental Plans with Orthodontic Coverage, and EyeMed Vision Insurance available to full-time employees. 403(B) Retirement Plan with a company match starting on day one for all full-time and part-time employees. Additional voluntary benefits including; Term and Whole Life Insurance, Accident Insurance, Critical Illness, Hospital indemnity, and Short-Term Disability. Flexible Spending Accounts, Dependent Care Accounts, Employee Assistance Program, Tuition Reimbursement and more. Primary Responsibilities: Conduct thorough HUD/DHCD HQS inspections of all SMOC RAPS existing units, potential new units, and the reinspection of those units as required including physical and remote virtual inspections. Verify unit compliance based on health and safety requirements. Verify unit conditions for rent reasonableness comparisons. Enter all inspection data into the MRI Tenmast Software Systems' Inspection module and monitoring information as needed; printing all required inspection-related letters for participating tenants and owners. Assist the Inspection Supervisor in providing "on the job" training for newly hired HQS inspectors in the field Assist the Inspection Supervisor in monitoring the various types of inspections conducted by the HQS Inspection team including remote virtual inspections, re-inspections, inspections conducted using an owner self certification and physical inspections Make recommendations to the Inspection Supervisor on behalf of the HQS inspectors on process and procedure Monitor HQS supplies and make requests to the Program Director on orders for necessary equipment such as gloves, shoe coverings and personal protective equipment as needed Utilize and maintain inspection-related equipment on a regular basis, including camera, hand-held inspection devices or tablets, flashlight, cell phone, tick tester, and inspection-supply cache. Engage all clients by understanding and addressing their needs whether within or outside the scope of work. Attend & participate in engagement team meetings as requested and communicate effectively with clients and staff in other areas. Maintain confidentiality of client, employee and agency information in accordance with federal and state laws and funder requirements. Ensure compliance with program/department, agency and/or funder requirements, as well as SMOC policies & procedures. Other duties as assigned. Knowledge and Skill Requirements: Education: High school diploma or equivalent Minimum years of related experience: 1-2 years preferred Knowledge of Excel, Windows, Word and PCs, ability to work well in a very high volume and productivity environment, ability to handle potentially stressful situations and sensitivity to the needs of economically- disadvantaged clientele. Valid Mass. driver's license and insurance Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Must meet all required DHCD program certifications within 1 year. Organizational Relationship: Directly reports to HQS Inspection Supervisor. Indirectly reports to Program Director, Assistant Director and Division Director. Direct reports of this position are none. Indirect reports of this position are HQS Inspectors. Physical Requirement: Physical effort required to do the job: Mobility to use office machines, sitting, standing, ability to lift archive boxes filled with files. Working Conditions: This job requires working in many different conditions and places. About 80% of the time is outside the office either on the road or at a tenant's unit. Therefore, conditions range from an office environment to an outdoor environment that can be dirty, wet, cold, hot, difficult and risky. As part of the responsibilities of this position, the Lead Inspector will have direct or incidental contact with clients served by SMOC in various programs funded or administered through the Executive Office of Health and Human Services. A successful background check is required.

Job DescriptionBenefits: 401(k) 401(k) matching Bonus based on performance Health insurance Resin Systems is a manufacturer of custom thermoset resin castings utilizing epoxy, urethane and silicone materials designed for highly dependable performance in hundreds of demanding applications and environments. Resin Systems creates components for a wide range of industries including Semiconductor, RF Microwave and Medical. Resin Systems Corporation is looking for talented individuals to support our continued growth. We have 1st shift positions available in our QC inspection department. Quality Inspector Responsibilities: - Conduct dimensional inspections on incoming materials, in-process production, and finished products from the various product lines as assigned by supervisor/management. - Use various measuring tools and equipment such as calipers, thread gages, pins and height gages to ensure product specifications are met - Perform visual inspections to identify any cosmetic defects or non-conformities - Perform cosmetic rework on identified minor cosmetic defects - Document and report inspection results and maintain accurate records - Follow established quality control (QC) procedures and guidelines Quality Inspector Skills: - Strong knowledge of quality control principles and practices - Proficiency in using measuring tools and equipment - Attention to detail and ability to identify defects or non-conformities - Excellent analytical and problem-solving skills - Familiarity with QC (Quality Control) processes - Ability to read and interpret technical drawings and specifications - Positive attitude and strong communication skills to collaborate with cross-functional teams - Must be willing to take initiative and be a self-starter Please note that this is not an exhaustive list of responsibilities and skills. Other duties may be assigned as needed by supervisor/management based on business requirements. Job Type: Full-time 8 hour shift Day shift Monday to Friday One location Ability to lift 50 lbs

At Plastic Distributors & Fabricators (PDF) , the Quality Inspector ensures that components and assemblies meet established quality standards and customer specifications. This role requires proficiency in operating and programming Coordinate Measuring Machines (CMM) and a strong working knowledge of Geometric Dimensioning and Tolerancing (GD&T). The Quality Inspector performs first article, in-process, and final inspections, utilizes precision measuring instruments, and partners closely with production and engineering teams to maintain and continuously improve product quality. Position Overview The Quality Inspector inspects parts and materials to ensure quality standards are maintained. This position verifies workmanship and compliance with specifications for piece parts and assemblies through dimensional and mechanical inspection methods. Key Responsibilities Inspection & Measurement Conduct inspections using precision measuring tools such as CMMs, micrometers, calipers, height gauges, and optical comparators Perform first article inspections (FAI), in-process inspections, and final inspections Accurately document inspection results and maintain records in accordance with quality management system requirements Technical Interpretation & Communication Interpret engineering drawings, blueprints, and specifications in accordance with GD&T Communicate inspection results and quality concerns to production, engineering, and quality teams Collaborate cross-functionally to resolve non-conformances and support corrective actions Quality Assurance & Continuous Improvement Ensure compliance with applicable quality standards and internal procedures Participate in internal audits and continuous improvement initiatives Support training of production personnel on quality requirements and inspection practices Perform other duties as assigned What You Bring (Core Competencies) Strong attention to detail and commitment to quality Analytical thinking and problem-solving skills Clear verbal and written communication skills Ability to work independently and as part of a team Flexibility to adapt to changing priorities and production demands Commitment to continuous learning and professional development Minimum Qualifications / Experience High school diploma or equivalent required Minimum of five (5) years of experience as a Quality Inspector in a manufacturing environment preferred Proficiency with Microsoft Office Suite Preferred Qualifications / Experience Bachelor's degree or technical certification in Quality Assurance, Plastics Machining, Manufacturing Technology, or a related field Knowledge of Statistical Process Control (SPC) and experience with capability studies Exposure to aerospace, life sciences, or defense manufacturing standards CCM experience Work Environment & Physical Requirements Ability to stand, walk, and perform repetitive movements for extended periods (8+ hours) Regularly lift, carry, and maneuver parts up to 25 pounds Manual dexterity to handle small parts, tooling, and precision measuring instruments Ability to wear required PPE, including safety glasses, safety shoes, gloves, and hearing protection Work in a manufacturing environment with moderate noise, temperature variation, and exposure to machining oils What We Offer Medical, dental, and vision insurance 401(k) with company match Paid time off and company holidays Special Requirements Employment is contingent upon successful completion of a reference check, criminal background check, and drug screening. Equal Employment Opportunity Evantic and its operating companies are equal opportunity employers. Qualified applicants will be considered for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, age, national origin, disability, veteran or military status, or any other characteristic protected by applicable law. The posted salary range is provided in accordance with applicable pay transparency requirements. Final compensation will be determined based on the candidate's qualifications, experience, skill set, internal equity considerations, and organizational needs

Acute Care TechnologySee attached Job Description At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary Verification of procured materials, sub-assemblies, finished products and processes to the companies Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Essential Functions Inspect measure and/or test material to established methods and standards. Utilize various inspection tools, such as Vision System, Verniers, Micrometers, Rulers, Oscilloscopes, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. Document inspection and test results according to established procedures. Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. Process returned material to established procedures. Read and interpret documentation such as Standard Operating Procedures (SOP), schematics, technical drawings, PDAs and ECOs. Interface with other functions and departments as required. Required/Preferred Education and Experience High School Diploma Or equivalent. required 1-3 years experience in a related position. required Knowledge, Skills and Abilities Good written and oral communication skills. Ability to read specifications, procedures and engineering drawings. Familiar with use of mechanical and electronic test equipment. IPC-A-61OD for Incoming Inspection, preferred. Basic computer skills: Microsoft Office, Oracle and MES. Physical Demands Ability to lift up to 50 lbs. ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. #LI-LV1 The hourly pay rate for this position is: $24.00 to $25.00 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

Rennscot MFG, founded in 2017, started as a motorsports-focused shop in the aftermarket automotive industry. Now, they are a leading provider of advanced manufacturing services located in Woburn, MA. Rennscot MFG strives to be more than just a machine shop; they solve problems in innovative ways, using a suite of integrated services to fuel a passion for ideation. With a focus on diversifying into commercial and critical technology sectors, Rennscot MFG delivers cutting-edge technologies and unwavering commitment to quality. They offer a comprehensive range of services, including reverse engineering, metal & polymer additive manufacturing, and precision machining to support various industries' needs. For more information, visit rennscotmfg.com. Description The Quality Control Inspector is responsible for ensuring that manufactured components meet engineering and customer specifications through precise inspection processes. This role places a strong emphasis on visual inspections, along with manual inspection methods, and requires a keen understanding of technical drawings and GD&T. Candidates will be considered for either an L1 (entry-level) or L2 (experienced) inspector position based on experience and qualifications. Responsibilities Operate pre-programmed CMM inspections (Zeiss/Calypso preferred) Load/unload parts and verify setups Interpret CMM results and compare them against engineering requirements Document findings in the MES (ProShop) and communicate deviations Perform manual inspections using a variety of precision metrology tools Calipers, micrometers, height gauges, thread gauges, bore gauges, etc. Visual inspections for defects such as nicks, scratches, and finish inconsistencies Review technical drawings and apply GD&T principles to inspections Conduct receiving, in-process, and final inspections Assist in non-conformance investigations, root cause analysis, and corrective actions Maintain accurate inspection records and ensure compliance with AS9100/ISO9001 standards Collaborate with machinists, engineers, and quality team members to resolve inspection-related concerns Adhere to company safety protocols, including proper PPE usage (eye protection, hearing protection, etc.) Step into other support roles as needed based on company demands; assist with CNC machine operation, post-processing additively manufactured parts, mechanical assembly, or logistics tasks (e.g., driving components to/from outside processing vendors) Required Skills & Qualifications Experience in quality inspection within a manufacturing environment Strong ability to interpret technical drawings, GD&T, and work instructions Proficiency in basic metrology tools (calipers, micrometers, etc.) Familiarity with non-conformance documentation and quality reporting Attention to detail and ability to work independently in a fast-paced environment Preferred Skills & Qualifications Experience running CMM programs (Zeiss/Calypso preferred) Ability to make minor adjustments to Calypso programs Understanding of statistical process control (SPC) and quality tools (FMEA, control plans, etc.) Experience working in regulated industries (aerospace, medical, automotive, etc.) Physical Demands Standing for extended periods Lifting/moving objects up to 50 lbs Fine motor skills for handling small precision components Working in an industrial environment requiring PPE (eye protection, hearing protection, etc.) ITAR Requirement To conform to US Government export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a US citizen, lawful permanent resident of the US, protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the US Department of State. Learn more about the ITAR here: **************************************************************************************** Rennscot MFG is an Equal Opportunity Employer; employment with Rennscot MFG is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

Life Science Outsourcing, Inc. (“LSO”) (**************** is a contract manufacturing organization focused on assembly, packaging, sterilization, and packaging with over 25 years of experience. The Company serves orthopedic, cardiovascular, diagnostic, dental and a variety of other medical specialties. Our unique model is focused on in-house end-to-end portfolio processes and service offerings with deep regulatory knowledge. This provides the agility and flexibility that customers need to accelerate their go-to-market launches while standardizing their supply chain and mitigating risk. Clients rely on LSO to perform all activities required to introduce their products to market, from procurement to final packaging and shipping. LSO's is headquartered in Brea, CA (North Orange County). In January 2023, the Company added its east coast facility in Somersworth, New Hampshire (formerly J-Pac Medical). We are currently seeking a self-motivated Customer Service Specialist with positive, engagement and collaborative energy to join our team and support the continued growth of the New Hampshire Facility. The Quality Inspector is responsible for quality assurance and quality manufacturing functions such as generating certificate of compliance, inspection and testing, disposition of product, incoming inspection, in-process and final inspection, review of DHRs (device history records). Qualifications Essential Duties and Responsibilities include the following: (NOTE: Other duties may be assigned) Following written procedures for testing and legibly and accurately documenting all test data. Communicate test data results and findings that are outside specified limits Maintaining compliance to appropriate US FDA regulations and ISO 13485 Quality Management System standards by following written procedures. Submitting and maintaining test result documents Working directly with manufacturing and engineering personnel to test and inspect components and materials Promoting the smooth flow of products through quality control to disposition Providing test and inspection support to all new process developments Reviewing Device History Records (DHR) Reviewing all lab results and approve product release. Working in a team environment with all quality control inspection personnel The ability to use manual dexterity to measure, using rulers, calipers, micrometers, and other instruments. Special projects as necessary Education and Experience High school degree or GED equivalent required. Not Required but preferred: 2 years of experience in a medical device manufacturing or pharmaceutical environment, or 5 years' experience in a general manufacturing environment. Knowledgeable in applications of caliper use, calibration and verification of tools, basic math skills and blueprints/drawings comprehension, IQ/OQ/PQ and quality principals. Basic knowledge of Good Manufacturing Practice. Basic knowledge in Quality Management Systems applicable to the medical device industry. Proficient in Microsoft Office Suite skills including electronic mail, record keeping, routine database activity, word processing, spreadsheets, graphics, etc. Skills and Abilities The Quality Inspector will have the following personal skills and attributes (in addition to the technical requirements for the job already mentioned): Attention to detail in a fast-paced environment Ability to work independently and take initiative Good interpersonal, communication (both verbal and written) Strong verbal and written communication skills Excellent organizational skills with the ability to handle multiple projects Passion for customer service and business growth Displays courtesy, tact and patience during interactions with all employees and customers Confident and creative Acts in an ethical manner at all times and demands the same in others Experience in process troubleshooting and timely resolution of issues. Eager to be a team player Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Individual will need to sit (at times for extended periods) or stand as needed. May require walking primarily on a level surface during the workday. Reaching above shoulder heights, below the waist or lifting as required to file documents or store materials during the workday.

Wave Life Sciences (Wave) is a biotechnology company focused on delivering transformational therapies for patients with serious, genetically defined diseases. We differentiate ourselves through our proprietary chemistry platform that enables the production of stereopure oligonucleotides precisely targeting the underlying cause of rare diseases. At Wave, we welcome those who share a passion to change lives and embrace a culture that is thoughtful, dynamic, humble, and fearless. Together, we can contribute to our mission enabling every patient with a genetic disease to have access to life-changing treatments. Description: Wave Life Sciences seeks a highly motivated and energetic chemistry, biochemistry, or chemical engineering major to join its Analytical/QC team in Lexington, Massachusetts. The co-op role will be responsible for routine testing and method development activities in support of process development, GMP production and clinical development. The position offers the opportunity to directly learn analytical methods and techniques that are in widespread use throughout the pharmaceutical and biotech industry. In addition, the co-op student will gain exposure to important functions of the development and manufacturing of pharmaceuticals, including analytics and stability, manufacturing processes and quality systems. A successful candidate will have hands-on experience with basic wet chemistry, sampling and testing organic or inorganic compounds, as well as other laboratory techniques. Experience with some of the following are a plus: HPLC, Karl Fischer moisture analysis, UV-Vis spectroscopy, microbiology testing, FTIR spectroscopy, chemical synthesis or purification processes. The candidate should also be able to adapt to a fast pace dynamic environment where priorities can change rapidly. This position is based in Lexington, MA at Wave's growing GMP manufacturing facility. Responsibilities: Perform analytical testing of in-process, finished product (API), raw materials Analyzes research and production samples Documentation and organization of data sets and reporting of results to other departments Troubleshoots analyses and assists in performance of investigations Assists in procurement and tracking of reagents and materials Reviews data generated by other analysts Executes method qualifications and validations Minimum Qualifications: Working towards a Bachelor's degree in chemistry or a related discipline (i.e. biochemistry, chemical engineering) At least two years of an undergraduate education completed within a related discipline. Intern must have successfully completed chemistry courses. Must possess excellent oral and written skills, as well as superior organizational skills. Analytical chemistry laboratory skills Analytical chemistry knowledge Competencies: Effective Communication Independence Flexibility/Adaptability to Change Accountability Teamwork Decision making EEO Statement: Wave Life Sciences provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Wave Life Sciences complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Wave Life Sciences expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Wave Life Sciences' employees to perform their job duties may result in discipline up to and including discharge. We value our relationships with professional recruitment firms. To protect the interests of all parties and given the large volume of inquiries received from third-party placement agencies, we are not able to respond to all agency inquiries. We do not accept unsolicited resumes from any source other than directly from candidates for current or future positions. Submission of unsolicited resumes in advance of a signed agreement between our company and a placement agency does not create an implied obligation and, if an unsolicited candidate represented by a placement agency is hired, we are not obligated to pay a fee. Only approved recruitment firms will be allowed to provide services to Wave Life Sciences, USA.

Job Description 1. Qualifications: a. High school diploma or GED required b. Minimum 3 years of relevant quality experience, within ISO13485/GMP manufacturing environment preferred, within extrusion is a plus c. Demonstrated efficiency and competency in core and advanced methods and gages for the inspection of tightly toleranced products d. Ability to read and interpret Engineering drawings e. Demonstrate initiative and self-motivation to create efficiencies and improve productivity within the inspection process f. Able to adapt and apply inspection knowledge to an array of product geometries and materials g. Work independently and prioritize assignments h. Will receive ongoing training to support competency and growth within the role i. Will receive opportunity and training to support growth within QC 2. Basic Position Skills: a. Organization - Able to react and maintain order and focus across shifting priorities and tasks b. Time Management - Able to balances multiple responsibilities and create efficiencies within the inspection process and achieve due dates c. Critical Thinking - Able to apply and adapt training and experience effectively to assigned tasks; ability to interact with data and identify risk d. Communication - Able to contribute across the team and coordinate with and support others to achieve departmental goals e. Mature work ethic - professional and positive attitude; provide constructive feedback and ownership to drive improvement within areas of responsibility 3. Reports to: Quality Supervisor 4. Primary job responsibility: The QC Inspector Level 2 is a mid-level position within the QC department for individuals who have demonstrated proficiency in all Level 1 competencies and responsibilities. The Level 2 Inspector utilizes core and advanced inspection methods and gages efficiently to perform inspections of extruded product across a broad range of product geometries and material to determine conformance to defined specifications. This position may include responsibility for an assigned Quality workflow and/or area of focus within an area of demonstrated expertise, efficiency and experience. 5. Essential functions of position: Perform Final Inspection for product Lot Release a. Prepare, follow, perform and document final inspections as defined on inspection paperwork for lot release b. Adapt inspection method techniques to accommodate the inspection of an array of products, including prototypes, profiles, multi-lumen and thin wall extruded tubes c. Demonstrate acceptable measurement error within inspection methods and techniques d. Assess conformance to defined specifications and requirements and identify and document non-conformance reports (NCR) e. Perform boundary inspections and actions as required to contain non-conforming product f. Complete thorough and detailed end-of-shift reporting Perform Start up and In-process inspection of manufacturing extrusion lines a. Prepare, follow and perform start-up and in-process inspections for multiple extrusion lines within a shift for an array of parts with varying degrees of difficulty relating to raw material properties, geometries, tolerances and methods b. React, adjust and communicate appropriately to challenges encountered during the extrusion process c. Identify and document non-conformances to defined specifications and requirements during the extrusion process d. Communicate inspection results and work with extrusion technician or operator to address non-conformances and at-risk product e. Identify, document, and perform boundary inspection to contain at-risk product encountered during the extrusion process Assigned Quality Workflow or Area of Focus a. Support assigned workflow or area of focus with accountability and action b. Create documented procedures and provide training as warranted c. Maintain appropriate documentation and tracking of workflow outcomes and performance as warranted d. Identify under performance and risk within the workflow and action needed to sustain and/or improve workflow outcomes and performance as warranted e. Coordinate and work with others as needed in support of assigned workflow f. Provide and maintain active communication and updates of assigned workflow to Quality Manager and/or Supervisor. Inspection Methods, Gages and Equipment a. Utilize pin gages, ring gages, calipers, rulers, vision systems, and other applicable gages as specified and within scope of training b. Utilize advanced inspection methods including automated OGP routines and advanced vision system techniques such as modeling and construction c. Recognize and respond to basic visual and dimensional quality indicators and erroneous data d. Create efficiencies within the inspection process e. Identify and report equipment and gages outside of calibration dates and exhibiting damage, wear, or malfunctions Documentation and Compliance f. Adhere to Good Documentation Practices (GDP) requirements g. Maintain accurate and complete records in all required documentation h. Follow defined processes and procedures appropriately and effectively identify gaps and/or misalignment with requirements i. Maintain product and lot traceability throughout the workflow and in all inspection documentation Safety and Housekeeping a. Follow all requirements and equipment safety procedures b. Identify and report safety hazards c. Keep work area clean and organized Communication a. Professional and courteous interactions b. Effective use of email and daily reporting to facilitate follow-up and action c. Proactive and constructive communication and support across the team to drive improvement and collaboration 6. Is the work described above checked by another individual? ? YES ? NO 7. Work Environment: a. Dynamic and fast-paced manufacturing floor, prone to interruptions b. Exposure to noise, high temperatures, moving machinery, and high-voltage equipment c. Clean room and gowning requirements Is the work described above checked by another individual? YES Consistent motor skills and other requirements of the position: Persistent: Standing: 10% Sitting: 75% Walking: 15% Consistent lifting of up to 35 lbs. - Rarely lifting of 1 lb. - Frequently Maximum carrying distance of up to 30 ft. - Occasionally Reaching - must be able to reach machines and/or materials up to 6 ft. from - Frequently Kneeling - N/A Climbing stairs - N/A Repetitive motion - right/left hand/wrist - Frequently Repetitive motion - right/left foot/ankle - N/A Continuous arm motions - Yes Must be able to avoid potentially moving which could cause injury - Yes Must be able to grasp and move object consistently and regularly - Yes Vision: intricate nature of work requires of 20/20 with or without corrective lenses - Yes Must be able to use gaging equipment and tools - Yes Must demonstrate to work productively and efficiently with others - Yes Microspec offers competitive wages and benefits, including: Sign-On Bonus Comprehensive Health Insurance Matching 401K plan annually after 1 year Entry-level 2 weeks paid vacation 64 Hours personal/sick time (unused time paid out at the end of the year) Annual discretionary bonus Salary range-$26.50-$28.00 per hour based on experience 20% Second Shift Differential